Modeling of the adsorption of a protein-fragment on kaolinite with potential antiviral activity

• Published in: Applied clay science Vol. 199; p. 105865
• Main Authors: Awad, Mahmoud E., Borrego-Sánchez, Ana, Escamilla-Roa, Elizabeth, Hernández-Laguna, Alfonso, Sainz-Díaz, C. Ignacio
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01-12-2020
• Subjects: Adsorption; Atmosfärsvetenskap; Atmospheric science; Glycoprotein E1; Hepatitis C virus; Hydration; Kaolinite; Molecular dynamics; Research Paper; Transmembrane domain; Virus sorption on minerals
• ISSN: 0169-1317; 1872-9053; 1872-9053
• DOI: 10.1016/j.clay.2020.105865

This work aimed at studying the potentiality of interactions between kaolinite surfaces and a protein-fragment (350–370 amino acid units) extracted from the glycoprotein E1 in the transmembrane domain (TMD) of hepatitis C virus capsid. A computational work was performed for locating the potential electrostatic interaction sites between kaolinite aluminol and siloxane surfaces and the residues of this protein-fragment ligand, monitoring the possible conformational changes. This hydrated neutralized kaolinite/protein-fragment system was simulated by means of molecular modeling based on atomistic force fields based on empirical interatomic potentials and molecular dynamic (MD) simulations. The MD calculations indicated that the studied protein-fragment interacted with the kaolinite surfaces with an exothermic process and structural distortions were observed, particularly with the hydrophilic aluminol surface by favorable adsorption energy. The viral units isolation or trapping by the adsorption on the kaolinite nanoparticles producing structural distortion of the peptide ligands could lead to the blockage of the entry on the receptor and hence a lack of viral activity would be produced. Therefore, these findings with the proposed insights could be an useful information for the next experimental and development studies in the area of discovering inhibitors of the global challenged hepatitis and other pathogenic viruses based on the phyllosilicate surface activity. These MD studies can be extended to other viruses like the COVID-19 interacting with silicate minerals surfaces.
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A protein of the Hepatitis C virus is adsorbed favorably on kaolinite surfaces.
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Adsorption on kaolinite provokes changes of Hepatitis C virus.
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Molecular dynamics are useful for exploring virus adsorption on mineral surfaces.